51461-07-5

Basic information

• Product Name: Benzenamine, 2,6-dimethyl-4-(phenylmethoxy)-
• CAS NO: 51461-07-5
• Molecular Formula: C15H17NO
• Molecular Weight: 227.306
• Mol File: 51461-07-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenamine, 2,6-dimethyl-4-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 2,6-dimethyl-4-(phenylmethoxy)-(51461-07-5)
• EPA Substance Registry System: Benzenamine, 2,6-dimethyl-4-(phenylmethoxy)-(51461-07-5)

Safety Data

• Hazardous Substances Data: 51461-07-5(Hazardous Substances Data)

Upstream product

• 4102-53-8 4-iodo-2,6-dimethylaniline 
• 100-51-6 benzyl alcohol 
• 87-62-7 2,6-dimethylaniline 
• 100-44-7 benzyl chloride 
• 5344-97-8 3,5-dimethyl-4-nitrophenol 
• 68657-15-8 5-(benzyloxy)-1,3-dimethyl-2-nitrobenzene 

Downstream Products

• 1307726-26-6 (E,E)-N,N'-(pyridine-2,6-diylbis(methanylylidene))bis(4-(benzyloxy)-2,6-dimethylaniline) 
• 17060-79-6 2-chloro-N-[2,6-dimethyl-4-(phenylmethoxy)phenyl]acetamide 
• 68657-16-9 4-benzyloxy-2,6-dimethylphenyl isocyanate 
• 103454-08-6 C₁₈H₂₂N₄O₂ 

Relevant articles and documents

Iron-catalyzed cycloaddition of alkynenitriles and alkynes

The combination of Fe(OAc)2 and an electron-donating, sterically hindered pyridyl bisimine ligand catalyzes the cycloaddition of alkynenitriles and alkynes. A variety of substituted pyridines were obtained in good yields.

Substituted phenyl amidinoureas

This invention relates to a method of lowering blood pressure in humans and mammals using 2,6-disubstituted phenyl amidinoureas in which the phenyl ring is additionally substituted by a hydroxy, alkoxy, aralkoxy, alkenyloxy, alkynyloxy, haloacyloxy, or acyloxy group and to novel 2,6-disubstituted phenyl amidinoureas which possess pharmaceutical properties, including blood pressure lowering activity.